Vaginal device

ABSTRACT

The present invention refers to a vaginal device  1  of an elastic material, said vaginal device  1  comprising a longitudinal portion  2  having a geometrical centre line  3 , an upper end  4  and a lower end  5  and which vaginal device  1  is intended to be inserted securely fixated inside of a vagina, the upper end  4  being the innermost of the vaginal device  1  in the vagina during use, to support against the urethra, through the vaginal wall, to prevent urinary stress incontinence in a woman, wherein the vaginal device  1  comprises at least one supporting portion  6  protruding from the longitudinal portion  2  and a reference member  7  protruding from the longitudinal portion  2  at the lower end  5 , which reference member  7  during use is fixated against the vaginal introitus, holding the vaginal device  1  securely fixated inside of the vagina and ensuring said at least one supporting portion  6  to support against the urethra.

FIELD OF THE INVENTION

The present invention relates to a vaginal device intended as an aid forwomen suffering from urinary stress incontinence.

BACKGROUND OF THE INVENTION

Urinary incontinence is a public health issue which affects more than 13million women in the USA only. There exist different types of urinaryincontinence in women, such as urge incontinence, stress incontinenceand mixed incontinence. Women having urge incontinence suffer from atleast some unwanted leakage caused by urgency. The focus herein ishowever not urge incontinence but urinary stress incontinence, oftenalso just called stress incontinence. Of the number of women sufferingfrom urinary incontinence about half of them suffer from stressincontinence. Urinary stress incontinence is mainly caused by connectivetissue laxity or damage in the vagina or its supporting ligaments. Thebackground to urinary stress incontinence and its origin may bedescribed by the Integral Theory (An integral theory and its method forthe diagnosis and management of female urinary incontinence, Petros P E,Ulmsten U I, Scand J Urol Nephrol Suppl, 1993; 153:1-93), which statesthat connective tissue damage to the 3 zones of the Integral System,which encompasses all three pelvic organs, bladder, vagina andano-rectum, is the ultimate cause of prolapse and dysfunction in theseorgans. In other words, stress incontinence may be caused by a defectfunction of the tissue or ligaments connecting the urethra and vaginalwall with the pelvic muscles and pubic bone. Examples of women sufferingfrom stress incontinence are such having experienced complicateddeliveries, such as disproportion, big child or instrumental delivery.However, genetic factors may also be of importance and may cause thesedefect functions.

Today there exist surgical methods supported by the knowledge of theIntegral Theory. For example, U.S. Pat. No. 5,899,909 discloses asurgical method for restoration of incontinence, the today called TVT(tension free vaginal tape) method which is a method effectivelypreventing and eliminating stress incontinence. U.S. Pat. No. 5,899,909discloses a method comprising the steps of passing a tape into the bodyvia the vagina first at one end thereof and then at the other endthereof at one side and the other, respectively, of urethra to form aloop around urethra, located between urethra and the upper vaginal wall,extending said tape over the pubic bone and through the abdominal wall,the ends of the tape being available outside the abdominal wall,tightening said strap at said ends, and leaving the tape implanted inthe body. The tape is left permanently in the body to provide itself, asan artificial ligament, the reinforcement of the tissue required inorder to restore the urinary incontinence, and/or to provide saidreinforcement by the development of fibrous tissue. A surgicalinstrument for performing the method according to U.S. Pat. No.5,899,909 is also disclosed.

The method disclosed according to U.S. Pat. No. 5,899,909 works verywell. However, it is a surgical method and as such it is not availablefor all women in need of help to reduce or eliminate stress incontinenceproblems. Due to the fact that stress incontinence in women is anextensive, widely spread problem all around the world, it is firstly notpossible to treat everyone in need of a surgical treatment. Secondly, inseveral countries, such as China and India, the possibility of receivinga TVT surgery is very limited. Moreover, many women suffering fromstress incontinence prefer conservative treatment or are not suitablefor TVT surgery, for instance due to high age. Furthermore, in countriesnot having free medical service, or with only parts of that servicebeing free, there will be many women having this problem but not thefinancial means to pay for a TVT surgery.

There exist today different devices with the purpose of alleviatingincontinence in women. U.S. Pat. No. 6,739,340 discloses a device forprevention of involuntary urination. The device comprises a body forarrangement in the vagina for compressive action on and support of theneck of the bladder and optionally the urethra. The body has asubstantially elongated shape with a longitudinal axis extending, in theintended direction of insertion, from a proximal to a distal end and ismade from a compressive and elastically deformable material. The bodycomprises at least one part protruding from the outer surface of thebody which is said to provide at least one pressure area for contactwith the neck of the bladder and optionally the urethra.

U.S. Pat. No. 6,645,137 discloses a vaginal insert having a flexiblebody either in the form of a belt or a split cylinder. In either case,the insert may be coiled into a coiled state. The body is said to have areduced diameter when coiled and exhibits a resilient bias towarduncoiling and expanding in diameter from the coiled state. When theinsert is inserted into the vagina of a patient, it is said to expandand press against the vaginal wall, such as for treating incontinence. Amedicament may be combined with the insert that is introduced to thepatient through contact with the insert, such as for treatingincontinence with a drug as well as pressure. The belt-type body mayincorporate mating ridges and grooves to keep the insert in acylindrical shape. Latch elements may be incorporated on the insert tosupport the insert in an expanded, partially uncoiled state.

There are disadvantages with the known vaginal devices disclosed above.Firstly, none of these devices are securely fixated inside of the vaginaduring normal use. When women move or for instance exercise there existsa great risk for movement of these devices inside the vagina. Anothercircumstance when this problem may be extensive is during a sneeze whenthe pressure power inside of the vagina is very large. This may alsorender the vaginal devices being pushed down towards the opening of thevagina. These cases of movement of the vaginal devices inside of thevagina render the pressing elements, that is the at least one protrudingpart in U.S. Pat. No. 6,739,340 and the protruding coils in U.S. Pat.No. 6,645,137, of the vaginal devices to press on the wrong site of thevaginal wall or urethra. In those cases these vaginal devices have onlylimited effect or no effect at all with respect to the prevention ofstress incontinence. Moreover, both of these devices may be harmful forthe patient or be perceived as unpleasant to use. This is caused by thedesigns of the pressing elements of these vaginal devices.

One object of the present invention is to provide a vaginal device forthe prevention of incontinence of the type called urinary stressincontinence, which vaginal device may function as an alternative for apatient not suitable for or one does not want to undergo a TVT surgeryand which vaginal device solves the problems described above with up tonow known vaginal devices.

SUMMARY OF THE INVENTION

The object above is solved by a vaginal device of an elastic material,said vaginal device comprising a longitudinal portion having ageometrical centre line, an upper end and a lower end and which vaginaldevice is intended to be inserted securely fixated inside of a vagina,the upper end being the innermost of the vaginal device in the vaginaduring use, to support against the urethra, through the vaginal wall, toprevent urinary stress incontinence in a woman, wherein the vaginaldevice comprises at least one supporting portion protruding from thelongitudinal portion, said at least one supporting portion beingintended to support against the urethra, through the vaginal wall, at asite located between close to the maximal urethral pressure point andthe bladder neck, and wherein the vaginal device also comprises areference member protruding from the longitudinal portion at the lowerend, which reference member during use is fixated against the vaginalintroitus, holding the vaginal device securely fixated inside of thevagina and ensuring said at least one supporting portion to supportagainst the urethra, through the vaginal wall, at the intended sitelocated between close to the maximal urethral pressure point and thebladder neck.

As is mentioned above, during use, said at least one supporting portionof the vaginal device according to the present invention is intended tosupport against the urethra, through the vaginal wall, at a site locatedbetween close to the maximal urethral pressure point and the bladderneck. The maximal urethral pressure point of the urethra is situatedclose to the middle point of the urethra or the mid urethra as it isalso called. When a woman is about to sneeze or cough, the pressurebuilt up along the urethra is the highest at this maximal urethralpressure point where the muscular pressure gets additional forces fromthe bending of the proximal portion of urethra in downward direction atthe “urethral knee”. The fixation of the distal portion of a normalurethra at the “urethral knee” is due to the support from the posteriorurethral ligaments on both sides of the urethra which connect thesymphysis pubis with the urethra and the anterior vaginal wall. Due tocompression of the urethra and a “curtsy effect” of the “urethral knee”during a pressure built up due to e.g. sneezing or coughing, this areais important to support so that the depression of the “urethral knee”decreases. This is accomplished by the at least one supporting portionof the vaginal device according to the present invention. Preferably,said at least one supporting portion according to the present inventionsupports against the urethra, through the vaginal wall, against themaximal urethral pressure point or very close to it. At this site, themaximal effect is obtained. According to the present invention, however,said at least one supporting portion may also support at sites betweenclose to the maximal urethral pressure point and the bladder neck, suchas at several sites. Moreover, the expression “close to the maximalurethral pressure point” should in this case be interpreted as possiblesites on both sides of the maximal urethral pressure point, and not onlyon that side facing towards the bladder neck.

The supporting portion of the vaginal device according to the presentinvention will support the lax urethra, through the vaginal wall, incases of stress incontinence caused by laxity of the posterior urethralligaments. In rest there will be no or very little compression of theurethra, which can interfere with the blood circulation. This is alsoimportant due to the fact that the vaginal device according to thepresent invention should be comfortable to use. This is also adifference in comparison to vaginal devices according to state of theart which are stated to press against the urethra through the vaginalwall. Furthermore, the at least one supporting portion according to thepresent invention must be designed to be able to support the urethra attimes when the pressure built up is very high, such as when a woman isabout to sneeze. This supporting feature of the vaginal device accordingto the present invention requires that the at least one supportingportion is flexible in its nature, both in terms of material andconstruction, but also able to support the urethra at the intended sitewhen the pressure wave along the urethra is large.

Another very important difference of the vaginal device according to thepresent invention in comparison to known devices is the reference memberof the present invention. The reference member protrudes from thelongitudinal portion at the lower end and is fixated against the vaginalintroitus. The reference member fixates the vaginal device in place sothat the at least one supporting portion supports the urethra at theintended site. This reference member is of great importance. When womenare moving there is an evident risk for vaginal devices to slide out ofplace inside of the vagina. In such a case, when and if a pressure wavearises from the abdomen, such as when sneezing or coughing, the vaginaldevice will not be fixated at the right place. This problem is solved bythe vaginal device according to the present invention, having thereference member making sure that the vaginal device and hence at leastone supporting portion to be fixated to support the urethra, through thevaginal wall, at the intended site.

Moreover, the fixation of the reference member against the vaginalintroitus is also of importance. The tissue against and around thevaginal introitus (labium minorae and majorae) shall be able to closearound the reference member, so that the reference member and vaginaldevice are fixated securely. This means that the fixation is made sothat the reference member is positioned at the labia minora, against thevaginal introitus, and not the labia majora. Due to the fact that labiamajora comprises fatty tissue and the size of the labia majora differs alot from woman to woman, it is difficult to design a reference memberfor fixation outside the labia majora. After the fixation, tight pair ofbriefs and possibly additional net pants will ensure that the fixatedvaginal device according to the present invention is secured in place.

The vaginal device according to the present invention may have differentdesign. For example, the at least one supporting portion does not haveto protrude around the longitudinal portion. It is, however, importantthat the at least one supporting portion of the vaginal device protrudesin the intended direction towards the urethra during use. As long as theat least one supporting portion is possible to support against theurethra, through the vaginal wall, the design thereof may vary. If thelongitudinal portion has a larger diameter it is possible to design thevaginal device so that the longitudinal portion in fact supports againstthe vaginal wall. In such a case, the at least one supporting portionshall not protrude in all directions from the longitudinal portion, thatis, shall not protrude around the longitudinal portion, due to the factthat the vaginal device as a whole in that case would not be able to beinserted in the vagina, or at least would not be comfortable to use. Insuch a case, the at least one supporting portion may e.g. have ahalf-moon shape or the like so that the supporting portion onlyprotrudes in an intended direction against the urethra. Many othershapes of the at least one supporting portion are also possible, such asflower-shaped and protruding around the longitudinal portion, protrudingaround the longitudinal portion asymmetrically, but of course also acircular shaped disc which hence protrudes symmetrically around thelongitudinal portion. In the latter case, the diameter of thelongitudinal portion of course is smaller in comparison with the case ofa half-moon shaped supporting portion due to the fact that the at leastone supporting portion protrudes around the longitudinal portion and assuch bears against the vaginal wall in all directions.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a side view of a vaginal device according to the presentinvention.

FIG. 2 shows a view of a vaginal device according to the presentinvention seen from the lower end of the longitudinal portion.

FIG. 3 shows a kit comprising a hollow vaginal device according to thepresent invention, seen from the side, as well as two different probesor rods which are introducible into the hollow vaginal device.

DETAILED DESCRIPTION OF THE INVENTION

As is mentioned above, the vaginal device according to the presentinvention is made of an elastic material. The degree of hardness ofmaterials possible to use for the vaginal device may be measured byshore A. Examples of possible materials may e.g. have a shore A of10-50, e.g. 10-40, 10-30, 20-40 or 20-30. According to another specificembodiment of the present invention, the vaginal device is made of anelastic material of medical quality, that is an inert material.Furthermore, the material may be roentgen visualised. The latter may beof interest so that the vaginal device is visible for X-ray examinationso that it is possible to see where the vaginal device according to thepresent invention supports the urethra, through the vaginal wall.Examples of possible elastic materials, that is elastic tissue acceptedinert materials, are polyurethane, silicone rubber, latex rubber,polystyrene copolymer materials and natural rubber, or combinationsthereof. Other elastic tissue accepted inert materials are of coursealso possible to use.

As is mentioned above, the design of the supporting portion according tothe present invention may vary, but the important characteristic of theportion is the supporting feature. According to one embodiment, the atleast one supporting portion is resilient in a radial direction towardsthe urethra through the vaginal wall. This implies that the supportingportion during support of the urethra, through the vaginal wall, mayfold itself somewhat in a radial direction, that is fold longitudinal tothe longitudinal portion. This may be of interest due to the fact thatthis may give an optimized support to the urethra without pressing tohard on the vaginal wall, and consequently the vaginal wall will not bedamaged by ischaemia. Moreover, it may also give an increased comfortfor the user in comparison to the known vaginal devices. The possibleradial resilience towards the urethra through the vaginal wall accordingto the present invention is also something that differs from the knownvaginal devices, which only may give resilience in an axial directiontowards the urethra through the vaginal wall. This may be observed bylooking at the drawings of U.S. Pat. No. 6,739,340, showing at least onerigid pressing member of the device which pressing member only isresilient due to use of a flexible material, as well as U.S. Pat. No.6,645,137, which discloses pressing rigid rings of a similar type as isdisclosed according to U.S. Pat. No. 6,739,340.

The at least one supporting portion according to the present inventionmay, however, also be of a more rigid type, such as the ones disclosedaccording to U.S. Pat. No. 6,739,340 and U.S. Pat. No. 6,645,137. Thechoice of the elastic material and the hardness thereof of the vaginaldevice are important in this sense. A thick at least one supportingportion is e.g. possible according to the present invention if a softelastic material having a low hardness (shore A) is chosen for thevaginal device. This gives a supporting portion which is not resilientin a radial direction towards the urethra through the vaginal wall, butdue to the choice of a soft elastic material, the supporting portionwill give both enough support to the urethra, through the vaginal wall,and still be harmless to the vaginal wall and comfort to use. The choiceof the design of the at least one supporting portion according to thepresent invention depends in other words on several parameters, such asif only one supporting portion is intended, the material of the vaginaldevice and hence supporting portion or portions and the thickness andmaterial thereof.

As mentioned above, the design of the at least one supporting portionmay vary. According to one specific embodiment of the present invention,the at least one supporting portion protrudes all around thelongitudinal portion. This implies that the at least one supportingportion or supporting member e.g. may look like flower-shaped or like acircular disc if the vaginal device is viewed from above. According toanother specific embodiment of the present invention, the at least onesupporting portion protrudes all around the longitudinal portion and issubstantially circular in a plane perpendicular to the geometricalcentre line. This implies a disc-like supporting portion disclosedabove.

Moreover, the vaginal device according to the present invention may beprovided with some specific features. According to one specificembodiment, the vaginal device of the present invention comprises atleast one perforation going through the at least one supporting portion.This at least one perforation may be provided as an outflow cavity forpossible menstrual blood inside of the vagina.

The size of the different parts of the vaginal device may vary. Forexample, the diameter of the vaginal device, especially at its widestplace, may vary. This is due to the fact that the size of vaginas ofwomen may vary. Therefore, according to one specific embodiment, the atleast one supporting portion protrudes all around the longitudinalportion, is substantially circular in a plane perpendicular to thegeometrical centre line and has a diameter of 25-45 mm, such as 25-40mm, 25-35 mm, 30-45 mm, 30-35 mm, 35-45 mm, 35-40 mm, 40-45 mm. Examplesof some possible diameters are 30, 35 and 40 mm. Although thisembodiment discloses at least one supporting portion or supportingmember being substantially circular, other shapes are possible as well,such as the flower-shaped supporting portion mentioned above. In such acase, the diameter should be interpreted as the length from a mostprotruding point of the supporting portion on one side of thelongitudinal portion to another most protruding point of the supportingportion on the other side of the longitudinal portion, through ageometrical centre inside of the longitudinal portion.

As said above, the diameter of the longitudinal portion may vary,dependent inter alia on if the supporting portion is protruding allaround the longitudinal portion. According to one specific embodiment ofthe present invention, the longitudinal portion is circular and has adiameter of 10-20 mm, such as 10-15 mm, 15-20 mm, e.g. 15 mm. Asubstantially circular cross section of the longitudinal portion isadvantageous due to the fact of a better fit inside of the vagina.

The length of the vaginal device may also vary. However, there exists alower possible threshold due to the fact that the vaginal device shouldmake it possible for the supporting portion to support at the possibleintended sites of the urethra. An upper limit exists also due to obviousreasons. This upper limit is about 90 mm due to the fact that the normallength of the vagina up to the anterior fornix is about that length inrest. According to one specific embodiment of the present invention, thelongitudinal portion has a length of 50-90 mm from the lower end to theupper end, such as 50-80 mm, 60-80 mm, e.g. 70 mm. According to oneembodiment, the upper end has a round shape and has a distance of 10-45mm to the uppermost of the at least one supporting portion, at thegeometrical centre line. This distance depends on the full length of thelongitudinal portion from the lower end to the upper end. According toyet another specific embodiment of the present invention, the distancefrom the lower end of the longitudinal portion to the centre of thelowermost of the at least one supporting portion, at the geometricalcentre line, is 20-55 mm, such as 20-50 mm, 20-45 mm, 20-40 mm, 20-35mm, 20-30 mm, 20-25 mm, 25-55 mm, 25-50 mm, 25-45 mm, 25-40 mm, 25-35mm, 25-30 mm, 30-55 mm, 30-50 mm, 30-45 mm, 30-40 mm, 30-35 mm, 35-50mm, 35-45 mm, 35-40 mm, 40-55 mm, 40-50 mm, 40-45 mm, 45-55 mm, 45-50mm, 50-55 mm, e.g. 20 mm, 25 mm, 30 mm, 35 mm, 40 mm or 45 mm.

The vaginal device according to the present invention may further beprovided with additional features. According to one embodiment, thelongitudinal portion is hollow from the lower end towards the upper end,but not through the upper end. This may be of interest when the vaginaldevice is intended to use in a kit together with some kind ofintroducible probe, rod or plug or the like, which should be possible toinsert into the cavity of the hollow vaginal device to give differentproperties. If the longitudinal portion is hollow, the wall of thelongitudinal portion, from the inside to the outside, should be thinenough so that the properties of the introducible probe, rod or plug orthe like is possible to afford to the vaginal device. As an example, ifthe introducible is a rod intended to give a higher hardness to thelongitudinal portion of the vaginal device, the wall of the vaginaldevice must be thin enough for the harder rod to give a high hardness tothe longitudinal portion.

Moreover, as said, the thickness of the at least one supporting portionmay vary. According to one embodiment of the present invention, the atleast one supporting portion has a thickness of 3-5 mm, such as 3-4 mm,4-5 mm, e.g. 4 mm. The thickness of the supporting portion is bydefinition the thickness in a direction which is perpendicular to theprotrusion of the supporting portion from the longitudinal portion.

According to the present invention, there may be provided more than onesupporting portion or supporting member along the longitudinal portion.Therefore, according to one specific embodiment of the presentinvention, the vaginal device comprises at least two supporting portionsprotruding from the longitudinal portion, said at least two supportingportions protruding separately from each other along the longitudinalportion and all of the at least two supporting portions being intendedto support against the urethra, through the vaginal wall, at siteslocated between close to the maximal urethral pressure point and thebladder neck. According to one embodiment of the present invention, thevaginal device comprises two supporting portions protruding from thelongitudinal portion, wherein the two supporting portions protrudeseparately from each other along the longitudinal portion. The distancebetween the two supporting portions or supporting members may in thisspecific case vary, but as an example the distance between these two maybe about 8-12 mm, such as 9-11 mm, such as about 10 mm, from ageometrical middle point of the uppermost supporting portion to ageometrical middle point of the lowermost supporting portion. Thisdistance corresponds to that of the vaginal tape used in a TVT surgery,and with two supporting portions which are resilient in a radialdirection towards the urethra through the vaginal wall, circularlyshaped and hence protruding around the entire longitudinal portion,these may together support the urethra, through the vaginal wall, at thesame site of the urethra as the TVT tape stabilises. To achieve thiseffect and to achieve an elevated resilient effect, it may beadvantageous to provide two supporting portions, in the shape ofcircular discs described above, which protrude separately from eachother along the longitudinal portion and which have a thickness of about4 mm. The diameter of these discs may e.g. be 30, 35 or 40 mm, thedistance from the lower end of the longitudinal portion to the lowermostof the two supporting portions may be 40-50 mm, such as 45 mm, along thegeometrical centre line, the distance between the lowermost of the twosupporting portions and the uppermost of the two supporting portions maye.g. be about 8-12 mm, such as 10 mm, from the geometrical centre of thelowermost of the two to the uppermost, at the centre line, and thedefined thickness of the two supporting portions may be 3-5 mm, such asabout 4 mm. Moreover, the longitudinal portion may be hollow as isdisclosed above.

According to one specific embodiment of the present invention, thevaginal device comprises two supporting portions protruding from thelongitudinal portion, said at least two supporting portions protrudingseparately from each other along the longitudinal portion and both ofthe at least two supporting portions being intended to support againstthe urethra, through the vaginal wall, at two sites located betweenclose to the maximal urethral pressure point and the bladder neck, andwherein the distance from the lower end of the longitudinal portion tothe centre of the lowermost of the two supporting portions, at thegeometrical centre line, is 20-50 mm, such as 25-45 mm, 30-45 mm, 35-50mm, 35-35 mm, e.g. 40 mm or 45 mm, and the distance from the lower endof the longitudinal portion to the centre of the uppermost of the twosupporting portions, at the geometrical centre line, is 50-65 mm, suchas 50-60 mm, e.g. 55 mm.

The design of the reference member according to the present inventionmay also vary. According to one specific embodiment, the referencemember has a right protruding end and optionally a left protruding end,the right protruding end protruding at least 40 mm from the geometricalcentre line of the longitudinal portion at the lower end and the leftprotruding end protruding below 25 mm, such as e.g. 10-25 mm, 10-20 mm,15-25 mm, e.g. 15 mm, from the geometrical centre line of thelongitudinal portion at the lower end. The meaning of the rightprotruding end and left protruding end of the reference member may beunderstood by viewing the accompanied drawings. The right protruding endof the reference member is that end that will be fixated against theperineum by the user, and if done, the left protruding end of thereference member is that end facing towards the opposite direction, thatis towards the clitoris but not reaching the same. This is the reasonfor the different length thresholds for the right and left protrudingend, respectively. About 40 mm or some above has proven to be afunctional length for the right protruding end of the reference memberfrom the centre line of the longitudinal portion so that the referencemember is possible to fixate against the perineum by the user in afunctional way. The left protruding end of the reference has asmentioned a length below 25 mm from the centre line of the longitudinalportion. This is due to that the left protruding end should be shortenough not to irritate the clitoris of a female user. However, even if avaginal device according to the present invention without a leftprotruding end of the reference member is possible, such a leftprotruding end may increase the stability and hence fixation of theentire vaginal device inside of the vagina during use. Without the leftprotruding end of the reference member there may be some risk for thevaginal device to sway and as such fall somewhat out of the perfectposition inside of the vagina, e.g. during substantial movement. Theshape of the right protruding end and left protruding end of thereference member may e.g. be ribbons which have widths that are smallerthan the diameter of the longitudinal portion.

According to one specific embodiment of the present invention, thereference member has a left protruding end and a right protruding end,the right protruding end protruding 40-50 mm from the geometrical centreline of the longitudinal portion at the lower end and the leftprotruding end protruding 10-25 mm from the geometrical centre line ofthe longitudinal portion at the lower end. 40-50 mm, such as 40-45 mm,45-50 mm, e.g. 45 mm, is a length interval of the right protruding endwhich may be suitable for an elevated fixation of the reference member.Moreover, 10-25 mm, such as 10-20 mm, 10-15 mm, 15-25 mm, 15-20 mm, e.g.15 mm, is a length interval of the left protruding end of the referencemember which is enough for achieving good fixation of the vaginal deviceinside of the vagina without any risk for any swaying during powerfulmovement by the user, but at the same time is short enough not toirritate the clitoris of the user. The reference member of the vaginaldevice according to the present invention functions as a means forinsertion and pulling out the vaginal device.

The shape of the reference member may vary, but a suitable example is asa ribbon which has the same width or a thinner width than thelongitudinal portion of the vaginal device according to the presentinvention. According to one specific embodiment, the reference member isconcave. This means that both of the right protruding end and leftprotruding end of the reference member may have this concave shape. Thepossible concave shape of the right protruding end and possibly also theshorter left protruding end means that these ends bend somewhat upwards,that is in a direction going from the lower end of the longitudinalportion and upwards. The bending or curvature in this case is not verylarge, and the length from the lower end of the longitudinal portion, atthe centre line, to a plane perpendicular to and intercepting thelongitudinal portion and the tip of the right protruding end, at thecentre line of the longitudinal portion, is about 5-30 mm, such as 10,15, 20 or 25 mm or in between thereof. This concave shape of thereference member may increase the stability and fixation of the vaginaldevice during use.

Furthermore, the vaginal device according to the present invention maybe provided with other additional features or means. According to onespecific embodiment of the present invention, a pressure sensor isprovided inside of the longitudinal portion at the upper end togetherwith means for expansion of the vaginal device situated inside of thelongitudinal portion. A pressure sensor may be provided together withmeans for expansion of the vaginal device so that when the pressureincreases inside of the vagina, the vaginal device will expand somewhatto take care of the pressure wave, such as during sneezing or coughing,and as such increase the support to the urethra at these pressureincreased situations. If a pressure sensor and means for expansion areprovided inside of the vaginal device, the pressure sensor should beprovided close to the upper end of the longitudinal portion so that thesensor will be able to sense an increase pressure wave coming from theabdomen as quick as possible. For example, the pressure sensor may beprovided just beneath an outer thin membrane which membrane constitutesthe surface of the vaginal device at the upper end thereof. The meansfor expansion may e.g. comprise an electromagnet and a coil. Theelectromagnet comprises an anchor and when an electric current isinduced in the coil due to a pressure increase detection by the pressuresensor, the anchor is moved and as such “kicks” the supporting portionso that this portion further supports the urethra, through the vaginalwall, at the intended site.

Moreover, if a pressure sensor is provided, it may be of interest tohave that provided inside of a longitudinal portion which hassubstantial length, in comparison, from the lower end to the upper, suchas up to 90 mm, due to the fact that in such a case the pressure sensorwill be situated to detect an increased pressure inside of the vagina asquick as possible. Moreover, the means for expansion of the vaginaldevice may be provided as different organs inside of the longitudinalportion, e.g. at least one organ situated inside of the longitudinalportion close to the at least one supporting portion so that theexpansion is made largest at the site or sites giving the most effectthereof.

As mentioned, the vaginal device according to the present invention maybe provided in a kit. According to one embodiment, there is provided akit comprising the vaginal device according to the present invention andat least one pharmaceutical agent. Examples of possible pharmaceuticalagents are oestrogen and alpha stimulators.

According to another specific embodiment, there is provided a kitcomprising a hollow vaginal device according to the present inventionand at least one introducible probe or rod matching the hollow vaginaldevice. The introducible plug, probe or rod may be of different type andhave different objects. The introducible plug or rod may be provided toincrease the diameter or hardness of the longitudinal portion. This maybe accomplished by introducing a rod of e.g. plastic material having ahigh hardness in comparison to the material of the rest of the vaginaldevice inside of the hollow longitudinal portion. The rod may in thiscase e.g. have a length which is the same as the length of the hole ofthe longitudinal portion or e.g. a bit shorter. The introducible plug,rod or probe should of course have a diameter which suits the diameterof the hole of the hollow longitudinal portion. Moreover, as said, thethickness of the wall of the hollow longitudinal portion should be thinenough so that the properties of the introducible plug, rod or probe arepossible to transfer to the longitudinal portion. The locking mechanismof the introducible rod, plug or probe, keeping it in place, may be ofdifferent sort, e.g. grooves on the rod, plug or probe that lock intorecesses provided inside of longitudinal portion at the lower endthereof.

Another possible introducible organ is a shorter plug, which mayfunction as a shock absorber inside of the hollow longitudinal portiondue to the fact that an air filled hole is provided between the tip ofthe plug and the upper end of the hollow longitudinal portion.

Moreover, the introducible rod or plug may also be possible to vibrate.The vibrating rod is e.g. provided with a battery and an on and offswitch for turning the vibration on and off. Another example of avibrating rod according to the present invention is a rod where thevibration is turned on automatically by contraction of the pelvis by auser, such as during pelvic floor training. Such a vibrating rod may beturned off automatically after e.g. 5-10 s when the contraction isdecaying. Such a vibrating rod may be an aid to facilitate muscletraining for the urethral zoon.

Moreover, the introducible rod or plug may be provided to release atleast one pharmaceutical agent which is intended to penetrate throughthe longitudinal portion of the vaginal device. In such a case, thelongitudinal portion should be of a membrane-like material which ispermeable for the intended at least one pharmaceutical agent.

According to another specific embodiment of the present invention, thereis provided a kit as above, wherein the introducible probe is a probefor electric nerve stimulation of the urethra and the pelvic floor. Theprobe is intended to provide stimulation through electrodes placed onthe longitudinal portion of the vaginal device or in combination withelectrodes situated on the centre or the supporting portions of thedevice. Preferably, the electrodes are situated in the periphery of thesupporting portions of the device. This stimulation should accomplishthe provision of electric pulses of low voltage and by a frequency e.g.in the range of from 5 to 50 Hz, such as 50 Hz. The polarity of thevoltage of the pulses should be shifted during the procedure and thereis a non-operating time between the different pulses. The pulses providea contraction of the urethral muscles which accomplish an increasedsupport/pressure against the urethra, through the vaginal wall. Due tothe fact that this stimulation gives a contraction of the urethralmuscles, the procedure provides not only a support but in fact also apressure on the urethra, through the vaginal wall and as such provides“automatic” perineal training. The electro-stimulation increases theurethral pressure and converts fast twitch fibers to slow twitch fibersin the striated muscles of the urethra during long term treatment. Slowtwitch fibers have the possibility to keep a contraction during longertime compared with the fast twitch fibers and will in that way resemblethe smooth muscles.

According to one specific embodiment of the present invention, there isprovided a kit comprising a hollow vaginal device according to thepresent invention and at least one introducible probe or rod matchingthe hollow vaginal device, the kit optionally comprising at least onepharmaceutical agent, wherein the at least one introducible probe or rodis a probe for electric nerve stimulation or a rod which may vibrate.

DETAILED DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a vaginal device 1 according to the present invention. Thevaginal device 1 comprises a longitudinal portion 2 having a geometricalcentre line 3, an upper end 4 and a lower end 5. Moreover, the vaginaldevice 1 comprises at least one supporting portion 6 protruding from thelongitudinal portion 2. In this case the vaginal device 1 according tothe present invention has two circular supporting portions 6, oneuppermost 8 having a centre 11 along the geometrical centre line 3 andone lowermost 10 having a centre 9 along the geometrical centre line 3,the supporting portions 6 protruding symmetrically around thelongitudinal portion 2. The vaginal device 1 also comprises a referencemember 7 protruding from the longitudinal portion 2 at the lower end 5.During use, the reference member 7 is fixated against the vaginalintroitus, holding the vaginal device 1 securely fixated inside of avagina and ensuring the two supporting portions 6 to support against theurethra, through the vaginal wall, at an intended site located betweenclose to the maximal urethral pressure point and the bladder neck,preferably located at the maximal urethral pressure point. In thisspecific case, the reference member 7 has a right protruding end 12 anda left protruding end 13, the right protruding end 12 being intended tobe fixated against the perineum by the user, and if done, the leftprotruding end 13 of the reference member is that end facing towards theopposite direction, that is towards the clitoris but not reaching thesame.

The vaginal device 1 according to the present invention shown in FIG. 1has a longitudinal portion having a circular cross section and adiameter of about 15 mm. Moreover, the diameters of the circularsupporting portions 6 are in this specific case 35 mm. The referencemember 7 is in this case concave and the right protruding end 12protrudes about 40 mm from the geometrical centre line 3 at the lowerend 5 of the longitudinal portion 2. The left protruding end 13 of thereference member 7 protrudes about 17.5 mm from the geometrical centreline 3 at the lower end 5 of the longitudinal portion 2. The referencemember 7 in this case is a ribbon which has a thickness perpendicular tothe geometrical centre line 3 of about 15 mm, that is the same thicknessas the diameter of the longitudinal portion 2. Furthermore, the distancefrom the lower end 5 to the centre 9 of the lowermost of the twosupporting portions 6, 10 is in this case about 45 mm along thegeometrical centre line 3. The distance between the two supportingportions, from centre 9 to centre 11, is about 10 mm. The distance fromthe centre 11 of the uppermost supporting portion 6, 8 to the roundupper end 4, at the geometrical centre line 3, is about 25 mm.

Naturally, the specific shapes and e.g. diameters of the different partsand portions of the vaginal device 1, and the distance between theseparts and portions, may vary, and the values given above should only beseen as examples.

FIG. 2 shows the vaginal device 1 according to FIG. 1, but seen frombelow, that is seen from the lower end 5. The longitudinal portion 2 isshown as a dashed circle in the middle.

FIG. 3 shows a kit according to the present invention. The kit in thiscase comprises a hollow vaginal device 1, which has the same shape asthe vaginal device according to FIG. 1, and two different types of rods14. The hollowness of the vaginal device 1 is shown by the dashed linegoing from the lower end 5 and up to the upper end 4, but not throughthe same. The rods 14 are of different type. One of them are long incomparison and is e.g. intended to increase the diameter and/or hardnessof the vaginal device 1 made of an elastic material of medical quality,to adjust the fit of the same inside of a vagina. The other rod 14 is ashorter plug, which may function as a shock absorber inside of thehollow longitudinal portion 2 due to the fact that an air filled hole isprovided between the tip of the plug and the upper end 4 of the hollowlongitudinal portion 2. There may of course be provided other types ofrods also in a kit according to the present invention, such as avibrating rod or a rod or plug 14 which may release at least onepharmaceutical agent which is intended to penetrate through thelongitudinal portion 2 of the vaginal device 1. Furthermore, it is e.g.also possible to provide an introducible probe which is a probe forelectric nerve stimulation of the urethra and the pelvic floor in a kitaccording to the present invention.

Pilot Study of Vaginal Devices According to the Present Invention

The effects of different vaginal devices or “vaginal plugs” according tothe present invention have been investigated on urinary stressincontinent women. First 8 women with urinary stress incontinence wereexamined with a vaginal device according to the invention having areference member in the form of a base plate protruding in alldirections from the longitudinal portion. The vaginal devices were madeof soft silicone rubber material of medical quality. Two different sizeswere used, called M35 and M40, both having a reference member as a plateprotruding outside the labia majorae and minorae in anterior-posteriordirection and having two supporting portions protruding separately fromeach other along the longitudinal portion and, said supporting portionsprotruding around the longitudinal portion and having circular crosssections in a plane perpendicular to the longitudinal portion, where thetwo different vaginal device had supporting portions with diameters of35 mm and 40 mm, respectively. The diameter of the longitudinal portionhaving a circular cross section was about 15 mm. The vaginal devices hadan upper end with a round shape and with a distance of about 15 mm tothe uppermost circular supporting portion, at the geometrical centreline. Moreover, the distance between the two supporting portions orsupporting members was about 10 mm at the geometrical centre line. Thefull length of the vaginal device, from the lower end to the upper endat the geometrical centre line, was about 70 mm.

As an effort to increase the fixation of the vaginal device, thereference member was cut giving a reference member, which no longer wasin the form of a base plate. Instead the new shape of the referencemember became a one side cut anchor ribbon actually only protruding in aright and left direction from the longitudinal portion, where e.g. theleft protruding end protruded a shorter distance from the geometricalcentre line than the right protruding end, or vice versa. The referencemember was still curved upward, just as the base plate, in the right andleft direction from the geometrical centre line. These cut versions ofthe vaginal device according to the invention was further used in theinvestigations.

Women with urinary stress incontinence were tested with this referencemember cut version of the vaginal device according to the presentinvention. 30 women were tested with the device having size M35, 2 womenwere tested with the device having size M40 and 1 woman was tested witha device having size M35 but not having a reference member at all. Thislast version is a device which is not intended to be part of the scopeaccording to the present invention and which may be seen as a comparingdevice. The lack of a reference member seemed to give an inferiorsupport of the mid-urethra compared with the cut version and wasabandoned.

Prior to the investigation, the women had been objectively diagnosed ashaving a genuine urinary stress incontinence by urodynamicinvestigation. No women with urge or mixed incontinence were included inthe investigation.

One woman of the 30 tested with the device of size M35 was excluded dueto the fact that the device was too wide and hence not possible toinsert into the vagina.

The test method was performed according to the following. After thewomen had given their oral consent, the vaginal device or plug wasinserted into the vagina together with some glide agent. A dryincontinence sanitary napkin was weighed. Thereafter the incontinencesanitary napkin was applied and was fixated with net pants. The women“springboard jumped” up and down 20 times with a full bladder, with legsgoing in an out. The leakage in the sanitary napkin was weighed on anelectronic weighing machine. The vaginal device according to the presentinvention was removed and a new incontinence sanitary napkin was weighedand applied. 20 new jumps were made in the same way as above. The secondsanitary napkin was weighed and the leakage with and without the vaginaldevice according to the present invention was calculated. Cystometricalbladder capacity was estimated before the test and registered andmicturated volume was notated after the test.

Results (Summary) of the Investigation of the 30 Women Tested for M35Type Device.

Below the results of the tests are summarised. As mentioned, one womanwas excluded because of a too narrow vagina for the M35 type device.

13 of the 29 women (45%) tested with the vaginal device obtained atotally dry incontinence sanitary napkin after the jump test;

26 of the 29 women (90%) obtained a reduced leakage when using thevaginal plug according to the present invention (comparison of theweight of the incontinence sanitary napkin when using the plug vs. notusing the plug after the jump test);

20 of the 29 women (69%) had at least a 50% leakage reduction;

the average reduction of the leakage was 58%;

Conclusions of the Performed Investigation

The vaginal device according to the present invention reduces the urineleakage in women suffering from urinary stress incontinence to a greatextent. In almost half the investigated cases the urine leakage waseliminated.

1. Vaginal device (1) of an elastic material, said vaginal device (1)comprising a longitudinal portion (2) having a geometrical centre line(3), an upper end (4) and a lower end (5) and which vaginal device (1)is intended to be inserted securely fixated inside of a vagina, theupper end (4) being the innermost of the vaginal device (1) in thevagina during use, to support against the urethra, through the vaginalwall, to prevent urinary stress incontinence in a woman, wherein thevaginal device (1) comprises at least one supporting portion (6)protruding from the longitudinal portion (2), said at least onesupporting portion (6) being intended to support against the urethra,through the vaginal wall, at a site located between close to the maximalurethral pressure point and the bladder neck, and wherein the vaginaldevice (1) also comprises a reference member (7) protruding from thelongitudinal portion (2) at the lower end (5), which reference member(7) during use is fixated against the vaginal introitus, holding thevaginal device (1) securely fixated inside of the vagina and ensuringsaid at least one supporting portion (6) to support against the urethra,through the vaginal wall, at the intended site located between close tothe maximal urethral pressure point and the bladder neck.
 2. Vaginaldevice (1) according to claim 1, wherein the vaginal device (1) is madeof an elastic material of medical quality.
 3. Vaginal device (1)according to claim 2, wherein the elastic material is chosen from thegroup consisting of polyurethane, silicone rubber, latex rubber,polystyrene copolymer materials and natural rubber, or combinationsthereof.
 4. Vaginal device (1) according to claim 1, wherein the atleast one supporting portion (6) is resilient in a radial direction. 5.Vaginal device (1) according to claim 1, wherein the at least onesupporting portion (6) protrudes all around the longitudinal portion(2).
 6. Vaginal device (1) according to claim 1, wherein the vaginaldevice (1) comprises at least one perforation going through the at leastone supporting portion (6).
 7. Vaginal device (1) according to claim 1,wherein the at least one supporting portion (6) protrudes all around thelongitudinal portion (2) and is substantially circular in a planeperpendicular to the geometrical centre line (3).
 8. Vaginal device (1)according to claim 1, wherein the at least one supporting portion (6)protrudes all around the longitudinal portion (2), is substantiallycircular in a plane perpendicular to the geometrical centre line (3) andhas a diameter of 25-45 mm.
 9. Vaginal device (1) according to claim 1,wherein the longitudinal portion (2) is circular and has a diameter of10-20 mm.
 10. Vaginal device (1) according to claim 1, wherein thelongitudinal portion (2) has a length of 50-90 mm from the lower end (5)to the upper end (4).
 11. Vaginal device (1) according to claim 1,wherein the upper end (4) has a round shape and has a distance of 10-45mm to the uppermost of the at least one supporting portion (8), at thegeometrical centre line (3).
 12. Vaginal device (1) according to claim1, wherein the distance from the lower end (5) of the longitudinalportion (2) to the centre (9) of the lowermost of the at least onesupporting portion (10), at the geometrical centre line (3), is 20-55mm.
 13. Vaginal device (1) according to claim 1, wherein thelongitudinal portion (2) is hollow from the lower end (5) towards theupper end (4), but not through the upper end (4).
 14. Vaginal device (1)according to claim 1, wherein the at least one supporting portion (6)has a thickness of 3-5 mm.
 15. Vaginal device (1) according to claim 1,wherein the vaginal device (1) comprises at least two supportingportions (6) protruding from the longitudinal portion (2), said at leasttwo supporting portions (6) protruding separately from each other alongthe longitudinal portion (2) and all of the at least two supportingportions (6) being intended to support against the urethra, through thevaginal wall, at sites located between close to the maximal urethralpressure point and the bladder neck.
 16. Vaginal device (1) according toclaim 15, wherein the vaginal device (1) comprises two supportingportions (6) protruding from the longitudinal portion (2), said at leasttwo supporting portions (6) protruding separately from each other alongthe longitudinal portion (2) and both of the at least two supportingportions (6) being intended to support against the urethra, through thevaginal wall, at two sites located between close to the maximal urethralpressure point and the bladder neck, and wherein the distance from thelower end (5) of the longitudinal portion (2) to the centre (9) of thelowermost of the two supporting portions (10), at the geometrical centreline (3), is 20-50 mm, and the distance from the lower end (5) of thelongitudinal portion (2) to the centre (11) of the uppermost of the twosupporting portions (8), at the geometrical centre line (3), is 50-65mm.
 17. Vaginal device (1) according to claim 1, wherein the referencemember (7) has a right protruding end (12) and optionally a leftprotruding end (13), the right protruding end (12) protruding at least40 mm from the geometrical centre line (3) of the longitudinal portion(2) at the lower end (5) and the left protruding end (13) protrudingbelow 25 mm from the geometrical centre line (3) of the longitudinalportion (2) at the lower end (5).
 18. Vaginal device (1) according toclaim 1, wherein the reference member (7) has a left protruding end (13)and a right protruding end (12), the right protruding end (12)protruding 40-50 mm from the geometrical centre line (3) of thelongitudinal portion (2) at the lower end (5) and the left protrudingend (13) protruding 10-25 mm from the geometrical centre line (3) of thelongitudinal portion (2) at the lower end (5).
 19. Vaginal device (1)according to claim 1, wherein the reference member (7) is concave. 20.Vaginal device (1) according to claim 1, wherein a pressure sensor isprovided inside of the longitudinal portion (2) at the upper end (4)together with means for expansion of the vaginal device (1) situatedinside of the longitudinal portion (2).
 21. Kit comprising the vaginaldevice (1) according to claim 1 and at least one pharmaceutical agent.22. Kit comprising a hollow vaginal device (1) according to claim 13 andat least one introducible probe or rod (14) matching the hollow vaginaldevice (1).
 23. Kit comprising a hollow vaginal device (1) according toclaim 13 and at least one introducible probe or rod (14) matching thehollow vaginal device (1), the kit optionally comprising at least onepharmaceutical agent, wherein the at least one introducible probe or rod(14) is a probe for electric nerve stimulation or a rod which mayvibrate.